Quick Links: Skip to main page content Skip to Search Skip to Topics Menu Skip to Common Links
  • Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

510(k) Premarket Notification
  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 


New Search Back To Search Results
Device Classification Name analyzer, gas, carbon-dioxide, gaseous-phase
510(k) Number K051857
Device Name VEO MULTIGAS MONITOR FOR POCKET PC, MODEL 400221
Applicant
WEISSBURG ASSOCIATES
4213 WINNEQUAH DRIVE
MADISON,  WI  53716
Applicant Contact DAVID WEISSBURG
Correspondent
WEISSBURG ASSOCIATES
4213 WINNEQUAH DRIVE
MADISON,  WI  53716
Correspondent Contact DAVID WEISSBURG
Regulation Number868.1400
Classification Product Code
CCK  
Subsequent Product Code
CCL  
Date Received07/08/2005
Decision Date 09/15/2005
Decision Substantially Equivalent (SESE)
Regulation Medical Specialty Anesthesiology
510k Review Panel Anesthesiology
Summary Summary
Type Traditional
Reviewed by Third Party No
Combination Product No
-
-